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Tumor vessel co-option: The past & the future
Anne Cuypers1, Anh-Co Khanh Truong1, Lisa M Becker1
1Laboratory of Angiogenesis and Vascular Metabolism, Center for Cancer Biology (CCB), Vlaams Instituut voor Biotechnologie (VIB) and Department of Oncology, Leuven Cancer Institute (LKI), KU Leuven, Leuven, Belgium.
Tumor vessel co-option (VCO) allows cancers to bypass anti-angiogenic therapy (AAT) by hijacking existing blood vessels. Novel technologies can uncover molecular mechanisms of VCO, revealing new therapeutic targets to overcome AAT resistance.
Area of Science:
- Oncology
- Cancer Biology
- Vascular Biology
Background:
- Tumor vessel co-option (VCO) is a non-angiogenic mechanism where tumors hijack host blood vessels.
- VCO is implicated in resistance to anti-angiogenic therapy (AAT), a common cancer treatment.
- The molecular drivers and cellular characteristics of VCO remain poorly understood.
Purpose of the Study:
- To review current knowledge on molecular mechanisms and models of VCO.
- To highlight recent sequencing-based studies on VCO.
- To propose future applications of novel technologies for VCO research.
Main Methods:
- Literature review of VCO mechanisms and models.
- Analysis of recent studies employing sequencing technologies (e.g., single-cell RNA sequencing).
- Discussion of emerging technologies for investigating tumor vascularization.
Main Results:
- VCO enables tumors to obtain blood supply independently of sprouting angiogenesis.
- Existing research on VCO, particularly using sequencing, is emerging.
- Novel technologies offer potential to elucidate VCO complexities.
Conclusions:
- Understanding VCO is crucial for overcoming AAT resistance.
- Advanced technologies like single-cell RNA sequencing can reveal VCO-specific endothelial cell (EC) biology.
- Future research using novel methods may identify vulnerabilities in VCO-dependent tumors, leading to new therapeutic strategies.
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